[EN] METHODS OF TREATING CANCERS<br/>[FR] MÉTHODES DE TRAITEMENT DE CANCERS
申请人:FOGHORN THERAPEUTICS INC
公开号:WO2021236080A1
公开(公告)日:2021-11-25
The present invention relates to methods and compositions for the treatment of BAF-related disorders such as acute myeloid leukemia. The present invention features methods to treat AML, e.g., in a subject in need thereof. In one aspect, the invention features a method of treating AML in a subject in need thereof, the method including administering to the subject an effective amount of an agent that reduces the level and/or activity of BRG1 and/or BRM.
Methods and compositions for diagnostic and therapeutic targeting of COX-2
申请人:Marnett J. Lawrence
公开号:US20070292352A1
公开(公告)日:2007-12-20
The presently disclosed subject matter provides compositions that selectively bind cyclooxygenase-2 and comprise a therapeutic and/or diagnostic moiety. Also provided are methods for using the disclosed compositions for diagnosing (i.e., by imaging) a target cell and/or treating a disorder associated with a cyclooxygenase-2 biological activity.
Amide exchange reaction: a simple and efficient CuO catalyst for diacetamide synthesis
作者:Qinghe Li、Peixue Wang、Youquan Deng
DOI:10.1039/c6ra05563j
日期:——
A highly copper-catalysed amide exchange reaction of hexamethylenediamine (HDA) with CH3CN and H2O for the synthesis of hexamethylenebisacetamide (HMBA) without an organic solvent or gas protection was developed. 100% HDA conversion and >99% HMBA selectivity was obtained. X-ray diffraction, scanning emission microscopy, and temperature-programmed reduction of hydrogen were used to characterize the
Der [M+11]<sup>+</sup>-Pik in den Massenspektren von Diaminen 38. Mitteilung über massenspektrometrische Untersuchungen
作者:Hardy Kühne、Manfred Hesse
DOI:10.1002/hlca.19820650521
日期:1982.7.28
The [M+ U]+-Peak in the Mass Spectra of Diamines
二胺类质谱中的[M + U] + -峰
Anodic oxidation of bisamides from diaminoalkanes by constant current electrolysis
作者:Tatiana Golub、James Y Becker
DOI:10.3762/bjoc.14.72
日期:——
monoamides upon anodicoxidation in methanol/LiClO4 because both types undergo majorly mono- and dimethoxylations at the α-position to the N atom. However, in cases where the spacer contains two methylene groups only the anodic process leads mostly to CH2-CH2 bond cleavage to afford products of type RCONHCH2OCH3. Moreover, upon replacing LiClO4 with Et4NBF4 an additional fragmentation type of product was generated